Ce Certification

What are the requirements for automotive parts and components to be allowed in the European market?

In Europe, the quality of your products is often measured by meeting specific requirements. Failure to fulfill or fail to meet these requirements will or will disrupt your attempts to find buyers in the European market.

1.  Requirements to meet

Type approval – Compliance with technical standards for motor vehicles

All Vehicle Type Approval  (WVTA) is a certificate for various types and types of motor vehicles. EU legislation has introduced strict conditions for the harmonization of technical, safety and environmental standards among EU Member States (vehicles) and for agricultural and forestry tractors.

This type of approval or certification is valid in all EU Member States and is necessary when you wish to sell your products in the EU. Many automotive components have not been approved until final assembly. In these cases, it is not necessary to certify individual components; however, these components will have to comply with the type-approval requirements.

In 2017 the testing process will change. In addition to the current laboratory emissions and fuel consumption tests (  New European Driving Cycle  ), a  Real Driving Emission  (RDE) test will be performed. Europe is also   contributing to the development of a new global testing system called the World Wide Harmonized Light Vehicle Testing Procedure (WLTP).


  • The Original Equipment Manufacturer and / or the approval authority determine the specific requirements that you must fulfill. These requirements vary widely per product and per market. This means that you may need to meet different requirements for different buyers and countries you export. Check the  specific type approval requirements of the receiver or approval authority for the parts you produce  .
  • An important requirement of the type approval certificate is the Production Eligibility (COP). COP, in conformity with the specification, performance and marking requirements in the product type validation legislation, refers to the ability to be produced in series which does not require another test. Make sure you have a suitable quality management system in place (see also dan Partner buyer requirements management section).

CE marking

Electronic equipment must be CE marked for marketing in the EU. The CE marking indicates that a product is assessed before it is placed on the market and meets EU safety, health and environmental protection requirements. The CE marking is sometimes also considered a means of conformity to the type-approval requirements; For example, electronic components requiring type approval and also electromagnetic compatibility (EMC) or CE marking for low-voltage equipment.


  •  Learn more about the type approval in the EU Export Help Desk  .
  •  Learn more about the CE marking of electrical equipment in the EU Export Help Desk  .
  •  Follow step-by-step guidance in CE marking  .
  • If you are an electronics or electrical engineering manufacturer in the automotive industry   take a look at our work on these issues .


To prevent environmental damage, the EU has restricted the use of certain chemicals in certain Regulations and Directives.


  • In most cases, it is your EU buyer who is responsible for complying with the legislation on chemicals. Share information with your buyer regarding the substances used in your product, thus proving that it complies with all relevant legislation.
  • Ask your buyer about the chemicals policies and their expectations. Sometimes these directions are called ”black / gray“ lists. Does it provide a list of items you cannot use or would you like to receive information about the substances you use in a certain way? If you don’t yet know your buyer, try looking at a chemicals policy for a car brand. For example, ‘calling Volvo REACH.
Ce Belgeleri

Why CE Marking?

The European CE marking regulation has been mainly set up to:

  • Harmonize all varying national regulations for consumer and industrial products in European Member States, so that the Single Market is encouraged;
  • Bring about cost savings for producers;
  • Enhance the safety of products;
  • Supply public bodies with a uniform procedure that can be checked.In the past, product requirements and test procedures in Europe were set by the individual Member States of the European Union. This meant that, for example, companies that wanted to sell their products on the European market sometimes had to deal with more than ten different technical requirements or procedures for just one product. The existence of all the different national legislation was contrary to the aim of the European Union in realizing one Single Market, in which there would be a free circulation of goods (as well as a free circulation of persons, services and capital).

CE marking Directives or ‘New Approach’ Directives

All the different product requirements brought many costs for the producers. With the help of the CE marking Directives or ‘New Approach’ Directives, the measures have been optimized by setting up European (European-wide) requirements, the harmonization of national legislation and directives, standards and mutual recognition of the technical standards, tests methods (compliance tests) and test laboratories, so that producers no longer need to adapt their products to the different markets.

In European countries, security and safety

During the process of harmonization the safety level of all products was attuned and raised. In most European countries, safety and health had already been the subject of directives for many years but the safety level was not always satisfactory.

With the help of the conformity assessment procedures, the authorities can ascertain that the products that are placed on the market comply with the requirements as stated in the regulations of the directives. The CE marking is consequently largely for the benefit of the authorities. However, safe products are also necessary for the end user in the work or consumer environment.

CE Certificate of Lighting

EGETEST CENTER LED / Lighting Luminaires CE Certificate / Marking works with qualified test laboratory.

EMC Tests for Lighting

LED / Lighting Fixtures must comply with the Low Voltage Directive and the Electromagnetic Compatibility Regulation.

LED / Lighting Luminaires must be subjected to LVD testing and reporting according to EN 60598-1 and related EN 60598-2-XX standard product specifications in accordance with the Low Voltage Directive .

EN 60598 Standard LED / is the standard series used in the certification process of lighting fixtures. It is used with a second party standard. This second party standard is determined by the purpose of the luminaire (eg EN 60598-2-5: Projectors) In general, the EN 60598 Standard series is as follows:

Standards and directives

  • TS EN 60598-1 Lighting fixtures – Part 1: General rules and tests
  • TS 8698 EN 60598-2-1 Lighting fixtures – Part 2: Special rules – Part one: General purpose, fixed
  • TS EN 60598-2-2 Lighting fixtures – Part 2: Particular requirements Part 2: Recessed fittings
  • TS 8700 EN 60598-2-3 Lighting fixtures – Part 2-3: Specific features – For road and street lighting
  • TS 8701 EN 60598-2-4 Lighting fixtures-Part 2: Special rules – Part 4: General purpose, portable
  • Lighting fixtures – Part 2: Special rules – Part 5: Projectors.


This standard covers the general characteristics of LED / Lighting fixtures operating with supply voltages up to 1000 V, combined with electrical light sources.

Another issue that should be considered is the Electromagnetic Compatibility Regulation.

TS EN 55015 Limit values ​​and measurement methods of radio distortion characteristics of electrical lighting and similar devices,

TS EN 61547 Devices used for general lighting purposes – Emu Immunity Rules

It must comply with its standards. The Low Voltage Directive for Lighting Products alone is not sufficient, but they must also comply with the Electromagnetic Compatibility Regulation.

LED / Lighting Fixtures Contact us for LVD and EMC Tests , we are in charge with our Test Laboratory.

CE Certificate for product

Harmonization of your Export Products to CE Standards

CE standardization, which is one of the basic obligations to be met in exports to the European Union; From elevator to toy, from construction materials to low-voltage appliances, from medical supplies to pressurized containers. The inclusion of commercial products, all of which have a wide range of different uses, and which have a wide range of qualifications, depends on the fact that the product meets CE standards, which is the minimum acceptable safety and compliance level.

How to get CE certificate?

The CE marking protocols may appear complex to inexperienced business owners, so the European Standards Committee on Standardization is defined briefly by CEN. Our firm, which eliminates such confusion in the process of applying CE certificate , provides consultancy and guidance on the execution of the application process in a way that will be completed in favor of the manufacturer in accordance with the legal regulations. Experienced and strict implementation of regulations, CE certificate applicationThanks to our team of experts who will ensure that the process is completed in minimum time and without any problems, getting a CE certificate for commercial enterprises becomes a simple job. Our engineering team informs you after completing the preliminary work on all necessary documents and works in a coordinated manner and advises you on how to eliminate deficiencies if needed. The technical file, which includes the studies related to all scientific research and legislation, has been approved by CEN, in other words, your application is made in such a way that you can obtain CE certificate by our organization which has completed its international accreditation.

Application Process for CE Certificate

In addition to the official documents containing the information on the legal status of the commercial enterprise that applies, as well as the signature file of the authorized or representative persons, the application file also contains the text of the agreement between the manufacturer and the firms that make the application. We help you in all matters such as creating records related to documents, preparing system documents, conducting required tests and investigations about products (LVD test, EMC test, etc.) in laboratory environment and conducting certification tests and we enable you to get CE approval without any problem. For all your inquiries about CE marking protocols and applications, just contact us.

Why the CE mark inside?

Thanks to the knowledge and experience of the Egetest Center expert teams for CE Marking, you will be able to sell your product to the European market without any problem. For detailed information and communication, send an email us or visit contact page for our online contact form.

CE Certificate Acquisition Process

With the expression of expert teams CE Certificate Acquisition Process

The companies that want to get CE Certificate should prepare technical files about the product they want to do first. The technical file that forms the basis of the CE Certificate tender process is required for all products that fall into the risky or risk-free category.

Companies that want to use CE marking must keep the technical file they prepared for the product throughout production. If a functional change is made to the product, the technical file must be refreshed. However, under all other conditions, the technical file must be stored for CE mark validity.

What information should be included in the technical file?

The technical file should contain the basic and technical information about the product to which the CE marking is to be received, as well as the information about the company. The information that should be included in the technical file is as follows:

  • Basic information about the company
  • Label or plate bearing the technical data of the product
  • What the product is used for
  • List of national and international standards used in the production of the product
  • Reports of these tests if you have the test made for the product
  • CE Declaration of Conformity
  • If the manufacturers of the electrical, hydraulic and pneumatic components of the product have been tested and approved by their code numbers and specifications and a competent body,certification about this,
  • Current operating instructions for the product
  • If the product’s supply list and supply products are covered by CE, certificates and test reports of these products
  • Detailed descriptions of how the product is installed, how it works and how the product is maintained.

If there is a deficiency in the technical file

The missing or defective information in the technical dossier will delay the process of obtaining the CE certificate, For this reason, companies must be careful when preparing technical files. It may also be necessary to pass tests such as LVC, EMI and EMC according to the category of the products to which CE certificate is requested. In this case, the technical file should include other tests and reports that should be used in electrical, electronic and telecommunication equipment.



CE Mark Usage Rights and Application Cost

CE standards, which represent the lowest level of production safety that can be accepted by the European Union, show that the product to be sold will have features that work in harmony with other products, systems and equipment in use.In accordance with the protocols established by the European Standardization Committee, the necessary tests and the preparation of the documents described in the legislation are organizations that provide assistance to manufacturers make applications for CE mark usage rights as businesses that have completed their international accreditation. The CE certificate fees requested by these authorities vary depending on which class the product is in which the manufacturer is applying for, and thus which inspections are requested for approval.

Producers who want to bring their products to the market in all member countries by taking advantage of free movement rights in the European Union receive CE certificate; means to prove that the product it produces is not harmful to human, environment and other living things. Although the producers are generally researched about the CE certificate prices that are requested by the authorized companies, our country is also involved in the adaptation process,Although the producers are generally researched about the CE certificate prices that are requested by the authorized companies, our country is also involved in the adaptation process, many private and public tenders today, CE marking standards in products even if the choice of compliance is not forgotten. and need to do research on indexing production to these standards. In the near future, the scope of products that need to bear CE marking is extended and all products may be required to meet these production safety and compliance standards. For those who want to export in EU countries, it is not optional to meet the CE marking standards.

CE certificate, which is not related to the legal entity of the company, may require additional application for each product depending on the characteristics and usage areas of the products produced. Planning such situations in advance Minimization of CE certificate prices and expenditures related to the overall cost of the application,the most economically advantageous decision for the company owners.Our firm offers attractive price options for consulting as well as CE certification to ensure that your applications are completed in a short time, without any hassle, and provide guidance on the necessary arrangements to ensure your product receives the right to use the CE marking. If you have questions about CE certificate fees, technical file preparation and application process, just contact us.